Kanegane Hirokazu | Departments Of Pediatrics Faculty Of Medicine Toyama Medical And Pharmaceutical University

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概要

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著作論文

ブルトン・チロシン・キナーゼの第1イントロンにおける転写調節異常
Open Heart Operation in a Child With Congenital Heart Disease and Hereditary Spherocytosis
Hepatocyte growth factor in transient myeloproliferative disorder of Down syndrome
Distinct Clones Are Associated with the Development of Transient Myeloproliferative Disorder and Acute Megakaryocytic Leukemia in a Patient with Down Syndrome
Outcome of Non-T-Cell-Depleted HLA-Haploidentical Hematopoietic Stem Cell Transplantation from Family Donors in Children and Adolescents
Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
Evans syndrome in a patient with Langerhans cell histiocytosis : possible pathogenesis of autoimmunity in LCH
Early lineage switch in an infant acute lymphoblastic leukemia
Pneumocystis jiroveci pneumonia as an atypical presentation of X-linked agammaglobulinemia
Spontaneous regression of aleukemic leukemia cutis harboring a NPM/RARA fusion gene in an infant with cutaneous mastosytosis
Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease
Acute lymphoblastic leukemia after living donor liver transplantation
Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients
Non-Hodgkin's Lymphoma of the Ascending Colon in a Patient with Becker Muscular Dystrophy : Report of a Case
Atypical X-linked Agammaglobulinemia Diagnosed in Three Adult
Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection
Atypical case of X-linked agammaglobulinemia diagnosed at 45 years of age
Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis

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